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血管紧张素原M235T基因多态性与肥厚型心肌病之间的关联。

Association between angiotensinogen M235T polymorphism and hypertrophic cardiomyopathy.

作者信息

Yao Jia-Lu, Sun Si-Jia, Zhou Ya-Feng, Xu Lang-Biao, Yang Xiang-Jun, Qian Xiao-Dong

机构信息

Department of Cardiology, The First Affiliated Hospital of Soochow University Suzhou 215006, Jiangsu, China.

出版信息

Int J Clin Exp Med. 2015 Jun 15;8(6):8767-75. eCollection 2015.

PMID:26309528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4538133/
Abstract

BACKGROUND

To investigate the relationship between angiotensinogen (AGT) gene M235T polymorphism and hypertrophic cardiomyopathy (HCM) to explore the potential role of the AGT polymorphism in HCM.

METHODS

PubMed, Embase, OVID, Cochrane library, CNKI, Wan Fang Database were searched to identify the studies involving AGT M235T polymorphism and HCM. Two authors performed independent literature review and study quality assessment using the Newcastle-Ottawa Scale (NOS) checklist. A random-effects model was used to calculate the overall combined risk estimates.

RESULTS

Nine studies involving 887 cases and 1407 controls were included in our meta-analysis. No significant associations were found between AGT M235T polymorphism and HCM (allele model T vs M: OR = 1.17, 95% CI = 0.95-1.45; dominant model TT vs (MM/MT): OR = 1.21, 95% CI = 1.00-1.45; recessive model (TT/MT) vs MM: OR = 1.12, 95% CI = 0.87-1.45; heterozygous comparison MT vs MM: OR = 1.07, 95% CI = 0.82-1.41; homozygous comparison TT vs MM OR = 1.19, 95% CI = 0.88-1.61. In subgroup analysis, the significant difference of association between AGT M235T polymorphism and HCM existed in Asian and sporadic hypertrophic cardiomyopathy (SHCM), but no significant difference was found in Europeans and familial hypertrophic cardiomyopathy (FHCM).

CONCLUSIONS

There is no association between AGT M235T polymorphism and HCM in general populations, but such a relationship exists in Asians and SHCM.

摘要

背景

研究血管紧张素原(AGT)基因M235T多态性与肥厚型心肌病(HCM)之间的关系,以探讨AGT多态性在HCM中的潜在作用。

方法

检索PubMed、Embase、OVID、Cochrane图书馆、中国知网、万方数据库,以识别涉及AGT M235T多态性和HCM的研究。两位作者使用纽卡斯尔-渥太华量表(NOS)清单进行独立的文献综述和研究质量评估。采用随机效应模型计算总体合并风险估计值。

结果

我们的荟萃分析纳入了9项研究,共887例病例和1407例对照。未发现AGT M235T多态性与HCM之间存在显著关联(等位基因模型T与M:OR = 1.17,95%CI = 0.95 - 1.45;显性模型TT与(MM/MT):OR = 1.21,95%CI = 1.00 - 1.45;隐性模型(TT/MT)与MM:OR = 1.12,95%CI = 0.87 - 1.45;杂合子比较MT与MM:OR = 1.07,95%CI = 0.82 - 1.41;纯合子比较TT与MM:OR = 1.19,95%CI = 0.88 - 1.61)。在亚组分析中,AGT M235T多态性与HCM之间关联的显著差异存在于亚洲人和散发性肥厚型心肌病(SHCM)中,但在欧洲人和家族性肥厚型心肌病(FHCM)中未发现显著差异。

结论

在一般人群中,AGT M235T多态性与HCM之间无关联,但在亚洲人和SHCM中存在这种关系。

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引用本文的文献

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Angiotensinogen M235T polymorphism and susceptibility to hypertrophic cardiomyopathy in Asian population: A meta analysis.血管紧张素原 M235T 多态性与亚洲人群肥厚型心肌病易感性的关系:荟萃分析。
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Renin-angiotensin system gene polymorphisms as potential modifiers of hypertrophic and dilated cardiomyopathy phenotypes.肾素-血管紧张素系统基因多态性作为肥厚型和扩张型心肌病表型的潜在修饰因素。
Mol Cell Biochem. 2017 Mar;427(1-2):1-11. doi: 10.1007/s11010-016-2891-y. Epub 2017 Jan 24.

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The M235T polymorphism of the angiotensinogen gene in South Indian patients of hypertrophic cardiomyopathy.南印度肥厚型心肌病患者血管紧张素原基因 M235T 多态性。
J Renin Angiotensin Aldosterone Syst. 2011 Sep;12(3):238-42. doi: 10.1177/1470320310387955. Epub 2010 Dec 16.
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